Mohapatra N, Lynn W S, Bhattacharyya S N
Biochem J. 1983 Sep 1;213(3):609-16. doi: 10.1042/bj2130609.
Tissues from rabbit lung were found to incorporate radioactivity from [3H]mannose into the oligosaccharide of a polar lipid soluble in chloroform/methanol/water (10:10:3, by vol.). Only one oligosaccharide-lipid was formed and the composition of the radiolabelled carbohydrate moiety was Glc3Man9(GlcNAc)2. An antitumour antibiotic, bleomycin, and an anti-inflammatory steroid, methylprednisolone, partially inhibited the incorporation of [3H]mannose into oligosaccharide-lipids and in addition resulted in the production of two new components, Man5(GlcNAc)2 and Man2(GlcNAc)2. Sodium dodecyl sulphate/polyacrylamide-gel electrophoresis of the glycoproteins synthesized from the oligosaccharide-lipid intermediates showed labelled components with Mr greater than 200000, 130000, 80000 and 62000. The addition of the drugs resulted in the same pattern with the addition of a new component of Mr 36000. Endoglucosaminidase H-treatment of the glycopeptides isolated from the Pronase-digested glycoproteins indicated that the oligosaccharide units in the glycoproteins were of the high-mannose-type.
研究发现,兔肺组织可将[³H]甘露糖中的放射性掺入一种可溶于氯仿/甲醇/水(体积比为10:10:3)的极性脂质的寡糖中。仅形成了一种寡糖脂质,放射性标记的碳水化合物部分的组成为Glc₃Man₉(GlcNAc)₂。一种抗肿瘤抗生素博来霉素和一种抗炎类固醇甲泼尼龙部分抑制了[³H]甘露糖掺入寡糖脂质中,此外还导致产生了两种新成分,即Man₅(GlcNAc)₂和Man₂(GlcNAc)₂。对由寡糖脂质中间体合成的糖蛋白进行十二烷基硫酸钠/聚丙烯酰胺凝胶电泳,结果显示标记成分的分子量大于200000、130000、80000和62000。添加药物后出现了相同的模式,同时还出现了一种分子量为36000的新成分。对从链霉蛋白酶消化的糖蛋白中分离出的糖肽进行内切葡糖胺酶H处理,结果表明糖蛋白中的寡糖单元为高甘露糖型。